Label: ACQUAINT ANTIBACTERIAL FOAM HANDWASH- chloroxylenol liquid
- NDC Code(s): 21749-551-90
- Packager: GOJO Industries, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated June 26, 2023
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- Active ingredient
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Inactive ingredients
Water (Aqua), Alcohol, Ammonium Laureth Sulfate, Ammonium Lauryl Sulfate, Propylene Glycol, Ammonium Xylenesulfonate, Cocamide MEA, Glycerin, Isopropyl Alcohol, Lactic Acid, Retinyl Palmitate, Simmondsia Chinensis (Jojoba) Seed Oil, Tetrasodium EDTA, Tocopheryl Acetate, Zea Mays (Corn) Oil, Ammonium Sulfate, Fragrance (Parfum), Methylchloroisothiazolinone, Methylisothiazolinone, Red 4 (CI 14700), Yellow 6 (CI 15985)
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INGREDIENTS AND APPEARANCE
ACQUAINT ANTIBACTERIAL FOAM HANDWASH
chloroxylenol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:21749-551 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL 0.003 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) AMMONIUM LAURETH-2 SULFATE (UNII: 698O4Z48G6) AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) AMMONIUM XYLENESULFONATE (UNII: 4FZY6L6XCM) COCO MONOETHANOLAMIDE (UNII: C80684146D) GLYCERIN (UNII: PDC6A3C0OX) ISOPROPYL ALCOHOL (UNII: ND2M416302) LACTIC ACID (UNII: 33X04XA5AT) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) JOJOBA OIL (UNII: 724GKU717M) EDETATE SODIUM (UNII: MP1J8420LU) .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N) CORN OIL (UNII: 8470G57WFM) AMMONIUM SULFATE (UNII: SU46BAM238) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) FD&C RED NO. 4 (UNII: X3W0AM1JLX) FD&C YELLOW NO. 6 (UNII: H77VEI93A8) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:21749-551-90 1250 mL in 1 PACKAGE; Type 0: Not a Combination Product 09/09/2004 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 09/09/2004 Labeler - GOJO Industries, Inc. (004162038) Establishment Name Address ID/FEI Business Operations GOJO Industries, Inc. 036424534 MANUFACTURE(21749-551) Establishment Name Address ID/FEI Business Operations GOJO Industries, Inc. 088312414 label(21749-551) , pack(21749-551)